Phe | |
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Salts [] | |
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Phenylalanine hydrochloride | |
Sodium phenylalanine | |
Molecular structure via molpic | |
| |
Molecular formula | C9H11NO2 |
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Molecular mass | 165.19 g/mol |
Predicted LogP | -1.5 |
Solubility | Soluble in water and dilute mineral acid and alkali hydroxide solutions |
Chirality | racemic |
Identifiers [] | |
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IUPAC name | 2-amino-3-phenylpropanoic acid |
SMILES | C1=CC=C(C=C1)CC(C(=O)O)N |
InChI | InChI=1S/C9H11NO2/c10-8(9(11)12)6-7-4-2-1-3-5-7/h1-5,8H,6,10H2,(H,11,12) |
InChIKey | COLNVLDHVKWLRT-UHFFFAOYSA-N |
Phenylalanine
Phenylalanine (also known as Dl-phenylalanine, DL-3-Phenylalanine, Phenylalanine DL-form, Phenylalanine, dl-, DL-2-Amino-3-phenylpropanoic acid, FEMA No. 3726, d,l-phenylalanine, CCRIS 8601, AI3-18436 or Phenylalanine dl) is a substance of the amino acid class.
Chemistry
Phenylalanine is typically found in the form of its hydrochloride and sodium salts.
Stereochemistry
DL-Phenylalanine is a racemic mixture of the logical stereoisomers:Stereoisomers [] | |
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D-Phenylalanine | L-Phenylalanine |
See also
External links
- Phenylalanine / D-Phenylalanine / L-Phenylalanine (Wikidata)
- Phenylalanine / D-Phenylalanine / L-Phenylalanine (PubChem)
- Phenylalanine / D-Phenylalanine / L-Phenylalanine (ChEMBL)
- Phenylalanine / D-Phenylalanine / L-Phenylalanine (ChEBI)
- Phenylalanine / D-Phenylalanine / L-Phenylalanine (Common Chemistry)
- Phenylalanine / L-Phenylalanine (HMDB)
- Phenylalanine / D-Phenylalanine / L-Phenylalanine (KEGG)
- Phenylalanine / D-Phenylalanine / L-Phenylalanine (UNII)
- Phenylalanine / D-Phenylalanine / L-Phenylalanine (EPA DSSTox)